Highly Sensitive Homogeneous Electrochemiluminescence Biosensor for Alkaline Phosphatase Detection Based on Click Chemistry-Triggered Branched Hybridization Chain Reaction

被引:24
作者
Huang, Xiaocui [1 ]
Bian, Xiangbing [2 ]
Chen, Lifen [3 ]
Guo, Longhua [3 ]
Qiu, Bin [1 ]
Lin, Zhenyu [1 ]
机构
[1] Fuzhou Univ, Coll Chem, Fujian Prov Key Lab Anal & Detect Food Safety, Minist Educ,Key Lab Analyt Sci Food Safety & Biol, Fuzhou 350116, Fujian, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Beijing 100039, Peoples R China
[3] Jiaxing Univ, Coll Biol Chem Sci & Engn, Jiaxing 314001, Zhejiang, Peoples R China
关键词
MESSENGER-RNA; IMMUNOASSAY; DNA;
D O I
10.1021/acs.analchem.1c02094
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Alkaline phosphatase (ALP) has been used as a diagnostic index of clinical diseases since its expression level is closely related to many pathological processes. In this work, a highly sensitive electrochemiluminescence (ECL) method for the determination of ALP based on a click chemistry-induced branched hybridization chain reaction (BHCR) for signal amplification and ultrafiltration technology for the separation of homogeneous amplification products is introduced. ALP can release copper ions from a Cu2+/PPi complex by hydrolyzing pyrophosphoric acid, which initiates click chemistry in the system. A BHCR amplification is triggered afterward by the long single-stranded DNA (ssDNA) generated by click chemistry, resulting in a three-dimensional double-stranded DNA (dsDNA) with a large molecular weight. Based on the characteristic that Ru(phen)(3)(2+) can stably insert into the groove of dsDNA, a large amount of Ru(phen)(3)(2+) is retained together with the amplified product after ultrafiltration, and therefore a significantly enhanced ECL signal can be obtained. The test results show that this method can be used for the quantitative determination of ALP ranging from 0.002 to 50 U/L, with a detection limit of 0.7 mU/L. This method has also been confirmed to have good selectivity and anti-interference, and the results of the analysis of the ALP content in the diluted serum samples are satisfactory, showing great application potential in clinical diagnosis.
引用
收藏
页码:10351 / 10357
页数:7
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